Functional Definition of Thyroid Hormone Response Elements Based on a Synthetic STARR-seq Screen.

Endocrinology

Institut de Génomique Fonctionnelle de Lyon, Université Claude Bernard Lyon I, CNRS UMR 5242, INRAE USC 1370 Ecole Normale Supérieure de Lyon, 69364 Lyon, France.

Published: August 2022

When bound to thyroid hormone, the nuclear receptor TRα1 activates the transcription of a number of genes in many cell types. It mainly acts by binding DNA as a heterodimer with retinoid X receptors at specific response elements related to the DR4 consensus sequence. However, the number of DR4-like elements in the genome exceed by far the number of occupied sites, indicating that minor variations in nucleotides composition deeply influence the DNA-binding capacity and transactivation activity of TRα1. An improved protocol of synthetic self-transcribing active regulatory region sequencing was used to quantitatively assess the transcriptional activity of thousands of synthetic sites in parallel. This functional screen highlights a strong correlation between the affinity of the heterodimers for DNA and their capacity to mediate the thyroid hormone response.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249314PMC
http://dx.doi.org/10.1210/endocr/bqac084DOI Listing

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